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An improved surface modification of poly(dimethylsiloxane) via a green chemistry approach for on-chip biomolecular separation

机译:通过绿色化学方法改进的聚二甲基硅氧烷表面改性,用于芯片上生物分子分离

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An enhanced facile strategy using a green chemistry method for the surface modification of poly(dimethylsiloxane) (PDMS) was developed via an in situ bulk free radical polymerization to resist nonspecific protein adsorption and to reduce electroosmotic flow (EOF). After silanization by 3-methacryloxypropyltrimethoxysilane, allyl-polyethylene glycol (PEG) was conjugated onto the PDMS surface with the aid of sodium persulfate. The surface properties of PDMS were characterized with Fourier transform infrared absorption by attenuated total reflection (ATR-FTIR) and contact angle experiments. EOF measurements and a nonspecific protein adsorption assay revealed a stable EOF suppression and remarkable protein-repelling properties for more than 30 days. Separation of FITC-labeled amino acids demonstrated a high reproducibility (migration time, RSD 2.2%). Further separation of fluorescence-labeled proteins using PDMS microchips before and after the surface modification showed that the PEG-modified PDMS microchip had an improved electrophoretic performance with a RSD of 1.49% for the migration time. In summary, a convenient strategy was developed for the modification of a PDMS microchip to prevent nonspecific protein adsorption and to enhance the electrophoretic performance. This improved environmentally friendly surface modification method will be useful for protein separation especially in batch production.
机译:通过原位本体自由基聚合反应开发了一种通过绿色化学方法对聚二甲基硅氧烷(PDMS)进行表面改性的增强型简便方法,以抵抗非特异性蛋白质吸附并减少电渗流(EOF)。在通过3-甲基丙烯酰氧基丙基三甲氧基硅烷进行硅烷化后,借助过硫酸钠将烯丙基聚乙二醇(PEG)共轭到PDMS表面。 PDMS的表面特性通过衰减全反射(ATR-FTIR)和接触角实验通过傅立叶变换红外吸收进行表征。 EOF测量和非特异性蛋白质吸附测定显示超过30天的稳定EOF抑制和非凡的蛋白质排斥特性。 FITC标记氨基酸的分离显示出高重现性(迁移时间,RSD为2.2%)。在进行表面修饰之前和之后,使用PDMS微芯片进一步分离荧光标记的蛋白质表明,PEG修饰的PDMS微芯片具有改善的电泳性能,迁移时间的RSD为1.49%。总之,开发了一种方便的策略来修饰PDMS微芯片,以防止非特异性蛋白质吸附并增强电泳性能。这种改进的对环境友好的表面修饰方法将对蛋白质分离特别是在批生产中有用。

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